US6071915A - Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia - Google Patents

Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia Download PDF

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Publication number
US6071915A
US6071915A US09/074,789 US7478998A US6071915A US 6071915 A US6071915 A US 6071915A US 7478998 A US7478998 A US 7478998A US 6071915 A US6071915 A US 6071915A
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United States
Prior art keywords
compounds
treatment
alkyl
compound
prostate
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Expired - Lifetime
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US09/074,789
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English (en)
Inventor
Linda Jolliffe
William Murray
Virginia Pulito
Allen Reitz
Xiaobing Li
Linda Mulcahy
Cynthia Maryanoff
Frank Villani
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ORCHO-MCNEIL PHARMACEUTICAL Inc
Janssen Pharmaceuticals Inc
Ortho Pharmaceutical Corp
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Ortho McNeil Pharmaceutical Inc
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Application filed by Ortho McNeil Pharmaceutical Inc filed Critical Ortho McNeil Pharmaceutical Inc
Priority to US09/074,789 priority Critical patent/US6071915A/en
Priority to MYPI98002108A priority patent/MY122095A/en
Priority to MYPI20041438A priority patent/MY127385A/en
Priority to ARP980102181A priority patent/AR012686A1/es
Priority to TW087107253A priority patent/TW512146B/zh
Assigned to ORTHO PHARMACEUTICAL CORPORATION reassignment ORTHO PHARMACEUTICAL CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LI, XIAOBING, REITZ, ALLEN, MARYANOFF, CYNTHIA, PULITO, VIRGINIA, VILLANI, FRANK, JOLLIFFE, LINDA, MULCAHY, LINDA, MURRAY, WILLAM
Assigned to ORCHO-MCNEIL PHARMACEUTICAL, INC. reassignment ORCHO-MCNEIL PHARMACEUTICAL, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: JOLLIFFE, LINDA, MARYANOFF, CYNTHIA, MULCAHY, LINDA, REITZ, ALAN, VILLANI, FRANK, MURRAY, WILLIAM, LI, XIAOBING, PULITO, VIRGINIA
Priority to US09/526,224 priority patent/US6890921B1/en
Application granted granted Critical
Publication of US6071915A publication Critical patent/US6071915A/en
Priority to US09/591,814 priority patent/US6593474B1/en
Priority to US10/452,255 priority patent/US20030220493A1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2632-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • C07D207/272-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2732-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
    • C07D207/277Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D207/282-Pyrrolidone-5- carboxylic acids; Functional derivatives thereof, e.g. esters, nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D211/74Oxygen atoms
    • C07D211/76Oxygen atoms attached in position 2 or 6
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D223/00Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/02Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D223/06Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D223/08Oxygen atoms
    • C07D223/10Oxygen atoms attached in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • C07D295/125Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/13Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain

Definitions

  • finasteride is a potent 5a-reductase inhibitor and causes a marked decrease in serum and tissue concentrations of dihydrotestosterone, it is only moderately effective in treating symptomatic BPH (Oesterling, 1995). The effects of finasteride take 6-12 months to become evident and for many men the clinical improvement is minimal (Barry, 1997).
  • R 1 is C 1-6 alkyl, phenyl,

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
US09/074,789 1997-05-12 1998-05-08 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia Expired - Lifetime US6071915A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
US09/074,789 US6071915A (en) 1997-05-12 1998-05-08 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
MYPI98002108A MY122095A (en) 1997-05-12 1998-05-09 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
MYPI20041438A MY127385A (en) 1997-05-12 1998-05-09 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperlasia
ARP980102181A AR012686A1 (es) 1997-05-12 1998-05-11 Un compuesto de piperazina aril-substituida, composicion farmaceutica que lo contiene y compuestos intermediarios utiles para la preparacion de dicha piperazina
TW087107253A TW512146B (en) 1997-05-12 1998-08-12 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
US09/526,224 US6890921B1 (en) 1997-05-12 2000-03-15 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
US09/591,814 US6593474B1 (en) 1997-05-12 2000-06-12 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
US10/452,255 US20030220493A1 (en) 1997-05-12 2003-06-02 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US4623697P 1997-05-12 1997-05-12
US09/074,789 US6071915A (en) 1997-05-12 1998-05-08 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia

Related Child Applications (1)

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US09/526,224 Continuation US6890921B1 (en) 1997-05-12 2000-03-15 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia

Publications (1)

Publication Number Publication Date
US6071915A true US6071915A (en) 2000-06-06

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Family Applications (4)

Application Number Title Priority Date Filing Date
US09/074,789 Expired - Lifetime US6071915A (en) 1997-05-12 1998-05-08 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
US09/526,224 Expired - Lifetime US6890921B1 (en) 1997-05-12 2000-03-15 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
US09/591,814 Expired - Lifetime US6593474B1 (en) 1997-05-12 2000-06-12 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
US10/452,255 Abandoned US20030220493A1 (en) 1997-05-12 2003-06-02 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia

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Application Number Title Priority Date Filing Date
US09/526,224 Expired - Lifetime US6890921B1 (en) 1997-05-12 2000-03-15 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
US09/591,814 Expired - Lifetime US6593474B1 (en) 1997-05-12 2000-06-12 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
US10/452,255 Abandoned US20030220493A1 (en) 1997-05-12 2003-06-02 Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia

Country Status (28)

Country Link
US (4) US6071915A (pt)
EP (1) EP0984777B1 (pt)
JP (1) JP4189867B2 (pt)
KR (1) KR100440755B1 (pt)
CN (3) CN1269807C (pt)
AP (1) AP1349A (pt)
AR (1) AR012686A1 (pt)
AT (1) ATE250033T1 (pt)
AU (1) AU7366998A (pt)
BR (1) BR9809804A (pt)
CA (1) CA2289987C (pt)
CZ (1) CZ298217B6 (pt)
DE (1) DE69818255T2 (pt)
DK (1) DK0984777T3 (pt)
EA (1) EA001904B1 (pt)
ES (1) ES2206928T3 (pt)
HK (1) HK1024630A1 (pt)
HU (1) HUP0100048A3 (pt)
IL (1) IL132836A0 (pt)
MY (2) MY122095A (pt)
NO (1) NO314144B1 (pt)
NZ (1) NZ500992A (pt)
PL (1) PL192596B1 (pt)
PT (1) PT984777E (pt)
TR (1) TR199902971T2 (pt)
TW (1) TW512146B (pt)
WO (1) WO1998051298A1 (pt)
ZA (1) ZA983968B (pt)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6248786B1 (en) * 1997-09-11 2001-06-19 Sanofi-Synthelabo Use of sulphonanilide derivatives to obtain a medicine for treating retrograde ejaculation or aspermia
WO2002022582A2 (en) * 2000-09-14 2002-03-21 Ortho-Mcneil Pharmaceutical, Inc. Solid salt forms of n-[2-[4-[2-(1-methylethoxy)phenyl]-1-piperazinyl]ethyl]-2-oxo-1-piperidineacetamide

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1346983A3 (en) * 1998-02-20 2003-12-03 Ortho-Mcneil Pharmaceutical, Inc. Phthalimido arylpiperazines as alpha 1A receptor antagonists useful in the treatment of benign prostatic hyperplasia
ZA991319B (en) * 1998-02-20 2000-11-20 Ortho Mcneil Pharm Inc Novel phthalimido arylpiperazines useful in the treatment of benign prostatic hyperplasia.
TW536538B (en) 1998-02-20 2003-06-11 Ortho Mcneil Pharm Inc Phthalimido arylpiperazines useful in the treatment of benign prostatic hyperplasia
EP1339682A1 (en) 2000-11-30 2003-09-03 Ranbaxy Laboratories, Ltd. 1,4-disubstituted piperazine derivatives useful as uro-selective $g(a)1-adrenoceptor blockers
WO2005118537A2 (en) * 2004-05-31 2005-12-15 Ranbaxy Laboratories Limited Arylpiperazine derivatives as adrenergic receptor antagonists
WO2006092710A1 (en) * 2005-03-02 2006-09-08 Ranbaxy Laboratories Limited Metabolites of 2-{3-[4-(2-isopropoxyphenyl) piperazin-1-yl]-propyl}-3a,4,7,7a-tetrahydro-1h-isoindole-1,3-(2h)-dione
WO2007029156A2 (en) * 2005-09-05 2007-03-15 Ranbaxy Laboratories Limited Isoindoledione derivatives as adrenergic receptor antagonists
CN102391169B (zh) * 2011-10-17 2015-10-28 上海化学试剂研究所 N-(5-甲氧基-3-吲哚乙基)-4-取代苯基哌嗪-1-乙酰胺的制备方法
CN103387531A (zh) * 2012-05-10 2013-11-13 广州医学院 酰胺类芳基哌嗪衍生物及其制备方法和在抗良性前列腺增生中的应用
CN103980195A (zh) * 2014-04-28 2014-08-13 广州医科大学 酰胺类苯基哌嗪衍生物及其盐与在制备治疗良性前列腺增生症药物中的应用

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4069336A (en) * 1976-02-25 1978-01-17 Chemisches Laboratorium Fritz-Walter Lange Gmbh & Co Kg (2-oxo-pyrrolidines)-acetic hydrazides
WO1984004302A1 (en) * 1983-04-27 1984-11-08 Byk Gulden Lomberg Chem Fab Substituted picolinic acids, processes for their preparation, their use and medicaments containing them
US4841051A (en) * 1985-12-10 1989-06-20 Nippon Kayaku Kabushiki Kaisha Phenylpiperazine derivatives
US5380725A (en) * 1988-05-24 1995-01-10 American Home Products Corporation Aryl- and heteroaryl piperazinyl carboxamides having central nervous system activity
US5403847A (en) * 1992-11-13 1995-04-04 Synaptic Pharmaceutical Corporation Use of α1C specific compounds to treat benign prostatic hyperlasia
US5807856A (en) * 1995-11-15 1998-09-15 Merck & Co., Inc. Alpha 1a adrenergic receptor antagonist

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5955878A (ja) 1982-09-24 1984-03-31 Chugai Pharmaceut Co Ltd 新規なフエニルピペラジン誘導体
GB8703749D0 (en) 1987-02-18 1987-03-25 Sandoz Ltd Piperazinecarboxylic acid
EP0558245A1 (en) * 1992-02-25 1993-09-01 RECORDATI S.A. CHEMICAL and PHARMACEUTICAL COMPANY Heterobicyclic compounds as antagogists of alpha-1 adrenergic and SHT1A receptors
FR2692894B1 (fr) * 1992-06-24 1994-10-14 Irceba Aryl-1-(o-alcoxy-phényl-4-pipérazinyl-1)-2, 3- ou 4-alcanols, leur procédé de préparation et leur utilisation pour la préparation de médicaments.
IT1266582B1 (it) * 1993-07-30 1997-01-09 Recordati Chem Pharm Derivati (di)azacicloesanici e diazacicloeptanici
US5688795A (en) * 1994-11-08 1997-11-18 Syntex (U.S.A.) Inc. 3-(4-phenylpiperazin-1-yl)propyl-amino, thio and oxy!-pyridine, pyrimidine and benzene derivatives as α1 -adrenoceptor antagonists
EP0881235A1 (fr) * 1997-05-26 1998-12-02 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Nouveaux ylures de phosphore, leur préparation et leurs utilisations notamment en tant que bases fortes faiblement nucléophiles
US6218396B1 (en) * 1998-02-20 2001-04-17 Orth-Mcneil Pharmaceutical, Inc. Substituted pyridino arylpiperazines useful in the treatment of benign prostatic hyperplasia
US6063785A (en) * 1999-02-17 2000-05-16 Ortho-Mcneil Pharmaceutical Inc. Phthalimido arylpiperazines useful in the treatment of benign prostatic hyperplasia
TW536538B (en) * 1998-02-20 2003-06-11 Ortho Mcneil Pharm Inc Phthalimido arylpiperazines useful in the treatment of benign prostatic hyperplasia

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4069336A (en) * 1976-02-25 1978-01-17 Chemisches Laboratorium Fritz-Walter Lange Gmbh & Co Kg (2-oxo-pyrrolidines)-acetic hydrazides
WO1984004302A1 (en) * 1983-04-27 1984-11-08 Byk Gulden Lomberg Chem Fab Substituted picolinic acids, processes for their preparation, their use and medicaments containing them
US4841051A (en) * 1985-12-10 1989-06-20 Nippon Kayaku Kabushiki Kaisha Phenylpiperazine derivatives
US5380725A (en) * 1988-05-24 1995-01-10 American Home Products Corporation Aryl- and heteroaryl piperazinyl carboxamides having central nervous system activity
US5403847A (en) * 1992-11-13 1995-04-04 Synaptic Pharmaceutical Corporation Use of α1C specific compounds to treat benign prostatic hyperlasia
US5807856A (en) * 1995-11-15 1998-09-15 Merck & Co., Inc. Alpha 1a adrenergic receptor antagonist

Non-Patent Citations (70)

* Cited by examiner, † Cited by third party
Title
Barry M., Roehrborn C. (1997) Management of Benign Prostatic Hyperplasia. Annual Review. 48: 177 188. *
Barry M., Roehrborn C. (1997) Management of Benign Prostatic Hyperplasia. Annual Review. 48: 177-188.
Breslin D, Fields DW, Chou T C, Marion DN, Kane M, Vaughan ED, and Felsen D (1993) Medical management of benign prostatic hyperplasia: a canine model comparing the in vivo efficacy of alpha 1 adrenergic antagonists in the prostate. J. Urol. 149: 395 399. *
Breslin D, Fields DW, Chou T-C, Marion DN, Kane M, Vaughan ED, and Felsen D (1993) Medical management of benign prostatic hyperplasia: a canine model comparing the in vivo efficacy of alpha-1 adrenergic antagonists in the prostate. J. Urol. 149: 395-399.
Bruno JF, Whittaker J, Song J, and Berelowitz M. (1991) Molecular cloning and sequencing of a cDNA encoding a human 1A adrenergic receptor. Biochem, Biophys. Res. Commun. 179: 1485 1490. *
Bruno JF, Whittaker J, Song J, and Berelowitz M. (1991) Molecular cloning and sequencing of a cDNA encoding a human α1A adrenergic receptor. Biochem, Biophys. Res. Commun. 179: 1485-1490.
Bylund DB, Eikenberg DC, Hieble JP, Langer SZ, Lefkowitz RJ, Minneman KP, Molinoff PB, Ruffolo RR, and Trendelenburg U (1994) IV. International Union of Pharmacology nomenclature of adrenoceptors. Pharmacol. Rev. 46: 121 136. *
Bylund DB, Eikenberg DC, Hieble JP, Langer SZ, Lefkowitz RJ, Minneman KP, Molinoff PB, Ruffolo RR, and Trendelenburg U (1994) IV. International Union of Pharmacology nomenclature of adrenoceptors. Pharmacol. Rev. 46: 121-136.
Carruthers SG (1994) Adverse effects of 1 adrenergic blocking drugs. Drug Safety 11: 12 20. *
Carruthers SG (1994) Adverse effects of α1-adrenergic blocking drugs. Drug Safety 11: 12-20.
Faure C, Gouhier C, Langer SZ, and Graham D (1995) Quantification of 1 adrenoceptor subtypes in human tissues by competitive RT PCR analysis. Biochem. Biophys. Res. Commun. 213: 935 943. *
Faure C, Gouhier C, Langer SZ, and Graham D (1995) Quantification of α1-adrenoceptor subtypes in human tissues by competitive RT-PCR analysis. Biochem. Biophys. Res. Commun. 213: 935-943.
Flavahan NA and VanHoutte PM (1986) 1 Adrenoceptor subclassification in vascular smooth muscle. Trends Pharmacol. Sci. 7: 347 349. *
Flavahan NA and VanHoutte PM (1986) α1-Adrenoceptor subclassification in vascular smooth muscle. Trends Pharmacol. Sci. 7: 347-349.
Ford APDW, Arredondo NF, Blue DR, Bonhaus DW, Jasper J Kava MS, Lesnick J, Pfister JR, Shieh IA, Vimont RL, Williams TJ, McNeal JE, Stamey TA, and Clarke DE (1996) RS 17053 (N 2 (2 Cyclopropylmethoxyphenoxy)ethyl 5 chloro a, a dimethyl 1H indole 3 ethanamine hydrochloride), a selective 1A adrenoceptor antagonist, displays low affinity for functional 1 adrenoceptors in human prostate: Implications for adrenoceptor classification. Mol. Pharmacol. 49: 209 215. *
Ford APDW, Arredondo NF, Blue DR, Bonhaus DW, Jasper J Kava MS, Lesnick J, Pfister JR, Shieh IA, Vimont RL, Williams TJ, McNeal JE, Stamey TA, and Clarke DE (1996) RS-17053 (N-[2-(2-Cyclopropylmethoxyphenoxy)ethyl]-5-chloro-a, a-dimethyl-1H-indole-3-ethanamine hydrochloride), a selective α1A-adrenoceptor antagonist, displays low affinity for functional α1-adrenoceptors in human prostate: Implications for adrenoceptor classification. Mol. Pharmacol. 49: 209-215.
Forray C, Bard JA, Wegzel JM, Chiu G, Shapiro E, Tang R, Lepor H, Hartig PR, Weinshank RL, Branchek TA, and Gluchowski C (1994) The 1 adrenergic receptor that mediates smooth muscle contraction in human prostate has the pharmacological properties of the cloned human 1c subtype. Mol. Pharmacol. 45: 703 708. *
Forray C, Bard JA, Wegzel JM, Chiu G, Shapiro E, Tang R, Lepor H, Hartig PR, Weinshank RL, Branchek TA, and Gluchowski C (1994) The α1-adrenergic receptor that mediates smooth muscle contraction in human prostate has the pharmacological properties of the cloned human α1c subtype. Mol. Pharmacol. 45: 703-708.
Gormley G, Stoner E, Bruskewitz RC et al. (1992) The effect of finasteride in men with benign prostatic hyperplasia. N. Engl. J. Med. 327: 1185 1191. *
Gormley G, Stoner E, Bruskewitz RC et al. (1992) The effect of finasteride in men with benign prostatic hyperplasia. N. Engl. J. Med. 327: 1185-1191.
Harrison JK, Pearson WR, and Lynch KR (1991) Molecular characterization of 1 and 2 adrenoceptors. Trends Pharmacol. Sci. 12: 62 67. *
Harrison JK, Pearson WR, and Lynch KR (1991) Molecular characterization of α1- and α2-adrenoceptors. Trends Pharmacol. Sci. 12: 62-67.
Hatano A, Takahashi H, Tamaki M, Komeyama T, Koizumi T, and Takeda M (1994) Pharmacological evidence of distinct 1 adrenoceptor subtypes mediating the contraction of human prostatic urethra and peripheral artery. Br. J. Pharmacol. 113: 723 728. *
Hatano A, Takahashi H, Tamaki M, Komeyama T, Koizumi T, and Takeda M (1994) Pharmacological evidence of distinct α1-adrenoceptor subtypes mediating the contraction of human prostatic urethra and peripheral artery. Br. J. Pharmacol. 113: 723-728.
Hieble JP and Caine M (1986) Etiology of benign prostatic hyperplasia and approaches to pharacological management. Fed. Proc. 45: 2601 2603. *
Hieble JP and Caine M (1986) Etiology of benign prostatic hyperplasia and approaches to pharacological management. Fed. Proc. 45: 2601-2603.
Hirasawa A, Horie K, Tanaka T, Takagaki K, Murai M, Yano J, and Tsujimoto G (1993) Cloning, functional expression and tissue distribution of human cDNA for the 1c adrenergic receptor. Biochem. Biophys. Res. Commun. 195: 902 909. *
Hirasawa A, Horie K, Tanaka T, Takagaki K, Murai M, Yano J, and Tsujimoto G (1993) Cloning, functional expression and tissue distribution of human cDNA for the α1c-adrenergic receptor. Biochem. Biophys. Res. Commun. 195: 902-909.
Holck MI, Jones CHM, and Haeusler G (1983) Differential interactions of clonidine and methoxamine with postsynaptic adrenoceptors of rabbit main pulmonary artery. J. Cardiovasc. Pharm. 5: 240 248. *
Holck MI, Jones CHM, and Haeusler G (1983) Differential interactions of clonidine and methoxamine with postsynaptic α-adrenoceptors of rabbit main pulmonary artery. J. Cardiovasc. Pharm. 5: 240-248.
Lepor H (1995) Blockade for benign prostatic hyperplasia (BPH) J. Clin. Endocrinol. Metab. 80: 750 753. *
Lepor H (1995) α-Blockade for benign prostatic hyperplasia (BPH) J. Clin. Endocrinol. Metab. 80: 750-753.
Lepor H and Rigaud G (1990) The efficacy of transurethral resection of the prostate in men with moderate symptoms of prostatism. J. Urol. 143: 533 537. *
Lepor H and Rigaud G (1990) The efficacy of transurethral resection of the prostate in men with moderate symptoms of prostatism. J. Urol. 143: 533-537.
Lepor H, Auerbach S, Puras Baez A et al. (1992) A randomized, placebo controlled multicenter study of the efficacy and safety of terazosin in the treatment of benign prostatic hyperplasia. J. Urol. 148: 1467 1474. *
Lepor H, Auerbach S, Puras-Baez A et al. (1992) A randomized, placebo-controlled multicenter study of the efficacy and safety of terazosin in the treatment of benign prostatic hyperplasia. J. Urol. 148: 1467-1474.
Marshall I, Burt RP, and Chapple CR (1995) Noradrenaline contractions of human prostate mediated by 1A ( 1c ) adrenoceptor subtype. Br. J. Pharmacol. 115: 781 786. *
Marshall I, Burt RP, and Chapple CR (1995) Noradrenaline contractions of human prostate mediated by α1A- (α1c-) adrenoceptor subtype. Br. J. Pharmacol. 115: 781-786.
Marshall I, Burt RP, Andersson PO, Chapple CR, Greengrass PM, Johnson GI, and Wyllie MG (1992) Human 1c adrenoceptor: functional characterization in prostate. Br. J. Pharmacol. 107(Proc. Suppl. Dec.):327P. *
Marshall I, Burt RP, Andersson PO, Chapple CR, Greengrass PM, Johnson GI, and Wyllie MG (1992) Human α1c-adrenoceptor: functional characterization in prostate. Br. J. Pharmacol. 107(Proc. Suppl. Dec.):327P.
Mebust WK, Holtgrewe HL, Cockett ATK, and Peters PC (1989) Transurethral prostatectomy: immediate and postoperative complication: a cooperative study of 13 participating institutions evaluating 3,885 patients.J. Urol. , 141: 243 247. *
Mebust WK, Holtgrewe HL, Cockett ATK, and Peters PC (1989) Transurethral prostatectomy: immediate and postoperative complication: a cooperative study of 13 participating institutions evaluating 3,885 patients.J. Urol. , 141: 243-247.
Minneman KP and Esbenshade TA (1994) 1 Adrenergic receptor subtypes. Annu. Rev. Pharmacol. Toxicol. 34: 117 133. *
Minneman KP and Esbenshade TA (1994) α1-Adrenergic receptor subtypes. Annu. Rev. Pharmacol. Toxicol. 34: 117-133.
Minneman KP, Han C and Abel PW (1988) Comparison of 1 adrenergic receptor subtypes distinguished by chloroethylclonidine and WB4101. Mol. Pharmacol. 33: 509 514. *
Minneman KP, Han C and Abel PW (1988) Comparison of α1-adrenergic receptor subtypes distinguished by chloroethylclonidine and WB4101. Mol. Pharmacol. 33: 509-514.
Morrow AL and Creese I (1986) Characterization of 1 adrenergic receptor subtypes in rat brain: A reevaluation of 3H WB4104 and 3H prazosin binding. Mol. Pharmacol. 29: 321 330. *
Morrow AL and Creese I (1986) Characterization of α1-adrenergic receptor subtypes in rat brain: A reevaluation of [3H]WB4104 and [3H]prazosin binding. Mol. Pharmacol. 29: 321-330.
Muramatsu I (1992) A pharmacological perspective of 1 adrenoceptors: subclassification and functional aspects, in Adrenoceptors (Fujiwara M, Sugimoto T, and Kogure K, eds.). Excerpta Medica Ltd., Tokyo, 193 202. *
Muramatsu I (1992) A pharmacological perspective of α1-adrenoceptors: subclassification and functional aspects, in α-Adrenoceptors (Fujiwara M, Sugimoto T, and Kogure K, eds.). Excerpta Medica Ltd., Tokyo, 193-202.
Muramatsu I, Oshita M, Ohmura T, Kigoshi S, Akino H, Gobara M, and Okada K (1994) Pharmacological characterization of 1 adrenoceptor subtypes in the human prostate: functional and binding studies. Br. J. Urol. 74: 572 577. *
Muramatsu I, Oshita M, Ohmura T, Kigoshi S, Akino H, Gobara M, and Okada K (1994) Pharmacological characterization of α1-adrenoceptor subtypes in the human prostate: functional and binding studies. Br. J. Urol. 74: 572-577.
Oesterling JE (1995) Benign prostatic hyperplasia. Medical and minimally invasive treatment options. N. Engl. J. Med. 332: 99 109. *
Oesterling JE (1995) Benign prostatic hyperplasia. Medical and minimally invasive treatment options. N. Engl. J. Med. 332: 99-109.
Price DT, Lefkowitz RJ, Caron MG, Berkowitz D, and Schwinn DA (1994) Localization of mRNA for three distinct 1 adrenergic receptor subtypes in human tissues: implications for human adrenergic physiology. Mol. Pharmacol. 45: 171 175. *
Price DT, Lefkowitz RJ, Caron MG, Berkowitz D, and Schwinn DA (1994) Localization of mRNA for three distinct α1-adrenergic receptor subtypes in human tissues: implications for human α-adrenergic physiology. Mol. Pharmacol. 45: 171-175.
Ramarao CS, Kincade Denker JM, Perez DM, Gaivin RJ, Riek RP, and Graham RM (1992) Genomic organization and expression of the human 1B adrenergic receptor. J. Biol. Chem. 267: 21936 21945. *
Ramarao CS, Kincade Denker JM, Perez DM, Gaivin RJ, Riek RP, and Graham RM (1992) Genomic organization and expression of the human α1B-adrenergic receptor. J. Biol. Chem. 267: 21936-21945.
Schwinn DA, Johnston GI, Page SO, Mosley MJ, Wilson KH, Worman NP, Campbell S, Fidock MD, Furness LM, Parry Smith DJ, Peter B, and Bailey DS (1995) Cloning and pharmacological characterization of human alpha 1 adrenergic receptors: sequence corrections and direct comparison with other species homologues. JPET 272: 134 142. *
Schwinn DA, Johnston GI, Page SO, Mosley MJ, Wilson KH, Worman NP, Campbell S, Fidock MD, Furness LM, Parry-Smith DJ, Peter B, and Bailey DS (1995) Cloning and pharmacological characterization of human alpha-1 adrenergic receptors: sequence corrections and direct comparison with other species homologues. JPET 272: 134-142.
Steers W., Zorn B. (1995) Benign Prostatic Hyperplasia, Disease a Month. vol. XLI No. 7 440 497. *
Steers W., Zorn B. (1995) Benign Prostatic Hyperplasia, Disease-a-Month. vol. XLI No. 7 440-497.
Weinberg DH, Trivedi P, Tan CP, Mitra S, Perkins Barrow A, Borkowski D, Strader CD, and Bayne M (1994) Cloning, expression and characterization of human adrenergic receptors 1A, 1B, and 1C. Biochem. Biophys. Res. Commun. 201: 1296 1304. *
Weinberg DH, Trivedi P, Tan CP, Mitra S, Perkins-Barrow A, Borkowski D, Strader CD, and Bayne M (1994) Cloning, expression and characterization of human α adrenergic receptors α1A, α1B, and α1C. Biochem. Biophys. Res. Commun. 201: 1296-1304.
Weis KA, Epstein RS, Huse DM, Deverka PA and Oster G (1993) The costs of prostatectomy for benign prostatic hyperplasia. Prostate 22: 325 334. *
Weis KA, Epstein RS, Huse DM, Deverka PA and Oster G (1993) The costs of prostatectomy for benign prostatic hyperplasia. Prostate 22: 325-334.
Wennberg JE, Roos N, Sola L, Schori A, and Jaffe R (1987) Use of claims data systems to evaluate health care outcomes: mortality and reoperation following prostatectomy. JAMA 257: 933 936. *
Wennberg JE, Roos N, Sola L, Schori A, and Jaffe R (1987) Use of claims data systems to evaluate health care outcomes: mortality and reoperation following prostatectomy. JAMA 257: 933-936.
Yamada S, Tanaka C, Kimura R, and Kawabe K (1994) Alpha 1 adrenoceptors in human prostate: characterization and binding characteristics of alpha 1 antagonists. Life Sci. 54: 1845 1854. *
Yamada S, Tanaka C, Kimura R, and Kawabe K (1994) Alpha 1-adrenoceptors in human prostate: characterization and binding characteristics of alpha 1-antagonists. Life Sci. 54: 1845-1854.

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US6248786B1 (en) * 1997-09-11 2001-06-19 Sanofi-Synthelabo Use of sulphonanilide derivatives to obtain a medicine for treating retrograde ejaculation or aspermia
WO2002022582A2 (en) * 2000-09-14 2002-03-21 Ortho-Mcneil Pharmaceutical, Inc. Solid salt forms of n-[2-[4-[2-(1-methylethoxy)phenyl]-1-piperazinyl]ethyl]-2-oxo-1-piperidineacetamide
WO2002022582A3 (en) * 2000-09-14 2002-10-17 Ortho Mcneil Pharm Inc Solid salt forms of n-[2-[4-[2-(1-methylethoxy)phenyl]-1-piperazinyl]ethyl]-2-oxo-1-piperidineacetamide

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